| Literature DB >> 28857359 |
Tetsuya Isaka1,2, Tomoyuki Yokose3, Yohei Miyagi4, Kota Washimi3, Teppei Nishii1, Hiroyuki Ito1, Haruhiko Nakayama1, Kouzo Yamada5, Munetaka Masuda2.
Abstract
It currently remains unclear whether tumor spread through airspaces (STAS) actually exist in vivo or are an artifact. The morphologies of STAS and tumor cell clusters in airway secretions collected from the segmental or lobar bronchus of resected lung adenocarcinomas and squamous cell carcinomas were compared among 48 patients. The EGFR status of tumor cell clusters in airway secretions was also compared with that of the main tumor in EGFR mutant adenocarcinomas. Tumor cell clusters were observed in the airway secretion cytology of ten patients (20.8%), and eight patients were adenocarcinoma (20.0% of adenocarcinoma). The morphology of STAS closely resembled that of tumor cell clusters detected in airway secretion cytology. The positive rates of airway secretion cytology were 83.3%, 100%, and 50% in papillary adenocarcinoma, micropapillary adenocarcinoma, and invasive mucinous adenocarcinoma, respectively. Among three EGFR mutant adenocarcinomas, the EGFR mutation subtypes of the main tumors in FFPE sections and tumor cell clusters in airway secretions were identical. These indicate that STAS may be detected in the airway secretion cytology. STAS is common in papillary or micropapillary adenocarcinoma and may spread as far as the segmental or lobar bronchus at the time of surgery.Entities:
Keywords: EGFR; STAS; adenocarcinoma; cytology; exon 19 deletion mutation; exon 21 L858R mutation; lung cancer; micropapillary
Mesh:
Year: 2017 PMID: 28857359 DOI: 10.1111/pin.12570
Source DB: PubMed Journal: Pathol Int ISSN: 1320-5463 Impact factor: 2.534